Peptide Imprinted Polymer Nanoparticles: A Plastic Antibody

被引:371
作者
Hoshino, Yu [1 ]
Kodama, Takashi [2 ]
Okahata, Yoshio [2 ]
Shea, Kenneth J. [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Tokyo Inst Technol, Dept Biomol Engn, Yokohama, Kanagawa 2268501, Japan
关键词
D O I
10.1021/ja8062875
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel method for preparation of biomacromolecular imprinted nanoparticles is described. Combinations of functional monomers were polymerized in the presence of the imprinting peptide melittin in aqueous solution at room temperature to produce a small library of polymer nanoparticles. The template peptide and unreacted monomers are subsequently removed by dialysis. Nanoparticles (NPs) from the library were evaluated for their binding to melittin by 27 MHz QCM analysis. NPs prepared with optimized functional monomer combinations bind strongly to the target molecule. Nanoparticles that were polymerized in the absence of template peptide were found to have little affinity to the peptide. Binding affinity and the size of imprinted particles are comparable to those of natural antibodies. They interact specifically with the target peptide and show little affinity for other proteins. These NPs are of interest as inert and stable substitutes for antibodies. Extension of this approach to other targets of biological importance and the applications of these materials are currently being evaluated.
引用
收藏
页码:15242 / +
页数:3
相关论文
共 25 条
[1]  
[Anonymous], 2004, MOL IMPRINTED MAT SC
[2]  
[Anonymous], 2001, MOL IMPRINTED POLYM
[3]   Structure and functions of channel-forming peptides: Magainins, cecropins, melittin and alamethicin [J].
Bechinger, B .
JOURNAL OF MEMBRANE BIOLOGY, 1997, 156 (03) :197-211
[4]  
Blondelle SE, 1996, J BIOL CHEM, V271, P4093, DOI 10.1074/jbc.271.8.4093
[5]   Molecularly imprinted polymers for the recognition of proteins: The state of the art [J].
Bossi, A. ;
Bonini, F. ;
Turner, A. P. F. ;
Piletsky, S. A. .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (06) :1131-1137
[6]   REVERSAL OF TOXICITY USING AVIDIN-BASED HEMOPERFUSION - A MODEL SYSTEM IN RATS USING BIOTINYLATED MELITTIN [J].
BRITT, AM ;
BURKHART, KK ;
BILLINGSLEY, ML .
PHARMACOLOGY, 1995, 50 (05) :307-312
[7]   Synthesis and characterization of pH-responsive copolymer microgels with tunable volume phase transition temperatures [J].
Debord, JD ;
Lyon, LA .
LANGMUIR, 2003, 19 (18) :7662-7664
[8]   A KINETIC-STUDY OF CONCANAVALIN-A BINDING TO GLYCOLIPID MONOLAYERS BY USING A QUARTZ-CRYSTAL MICROBALANCE [J].
EBARA, Y ;
OKAHATA, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (25) :11209-11212
[9]  
GRUNIGEN RV, 1989, IMMUNOLOGY, V66, P339
[10]   BEE WASP VENOMS [J].
HABERMAN.E .
SCIENCE, 1972, 177 (4046) :314-+